A growing body of evidence indicates that IgA1 present in the serum of patients with IgA nephropathy (IgAN) displays aberrant structural properties in its carbohydrate side chains. Increased serum levels of IgA1 may be related to the recently shown deficient galactosyation of IgAN IgA1 demonstrated by lectin-binding studies and direct analyses of igA1 isolated from sera of IgAN patients. This galactose (Gal) deficiency appears to be restricted to the hinge region of glycans of IgA1, which are primarily responsible for interactions with the asialoglycoprotein receptor (ASGP-R) and catabolism of IgA1 by hepatocytes. The absence of Gal exposes the new terminal sugar. N-acetylgalactosamine (GalNAc) as demonstrated by an increased reactivity of serum IgA1 from patients with IgAN GalNAc-specific lectins. The possible relationship between the aberrant glycosylation of IgA1 and IgAN was indicated by an observation which demonstrated the presence of a receptor on human mesangial cells that binds but does not internalize degalactosylated IgA1. In this project, we propose to test the following hypothesis: Gal-deficiency of a small population of IgA1 molecules (due to the functional deficeincy of beta 1-3 galactosyltransferase [Beta 1-3GT] in IgA1-producing cells of patients with IgAN), leads to alterations in their elimination from the circulation and their liver catabolism, and results in their deposition in kidney mesangia. The overall goal is to determine if the aberrant glycosylation of IgA1 is the underlying cause of IgAN. In addition to providing potential diagnostic procedures for the early identification of children at risk for the development of IgAN, these studies may suggest a rational basis for the design of effective therapeutic approaches. This project will obtain serum samples from 50 healthy adults to use as control samples in studies of the molecular abnormalities of immuno- globulin A in IgA nephropathy. Prospective subjects are screened by a brief physical examination and questionnaire before a 20-ml venous blood sample is drawn.

Project Start
Project End
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Yu, Alan S L; Shen, Chengli; Landsittel, Douglas P et al. (2018) Baseline total kidney volume and the rate of kidney growth are associated with chronic kidney disease progression in Autosomal Dominant Polycystic Kidney Disease. Kidney Int 93:691-699
Askie, Lisa M; Darlow, Brian A; Finer, Neil et al. (2018) Association Between Oxygen Saturation Targeting and Death or Disability in Extremely Preterm Infants in the Neonatal Oxygenation Prospective Meta-analysis Collaboration. JAMA 319:2190-2201
McKenzie, Katelyn A; El Ters, Mirelle; Torres, Vicente E et al. (2018) Relationship between caffeine intake and autosomal dominant polycystic kidney disease progression: a retrospective analysis using the CRISP cohort. BMC Nephrol 19:378
Srinivasan, Lakshmi; Page, Grier; Kirpalani, Haresh et al. (2017) Genome-wide association study of sepsis in extremely premature infants. Arch Dis Child Fetal Neonatal Ed 102:F439-F445
Morrison, Shannon A; Goss, Amy M; Azziz, Ricardo et al. (2017) Peri-muscular adipose tissue may play a unique role in determining insulin sensitivity/resistance in women with polycystic ovary syndrome. Hum Reprod 32:185-192
Shen, Chengli; Landsittel, Douglas; Irazabal, María V et al. (2017) Performance of the CKD-EPI Equation to Estimate GFR in a Longitudinal Study of Autosomal Dominant Polycystic Kidney Disease. Am J Kidney Dis 69:482-484
Denson, Lee A; McDonald, Scott A; Das, Abhik et al. (2017) Early Elevation in Interleukin-6 is Associated with Reduced Growth in Extremely Low Birth Weight Infants. Am J Perinatol 34:240-247
Kline, Timothy L; Korfiatis, Panagiotis; Edwards, Marie E et al. (2017) Image texture features predict renal function decline in patients with autosomal dominant polycystic kidney disease. Kidney Int 92:1206-1216
James, Jennifer; Munson, David; DeMauro, Sara B et al. (2017) Outcomes of Preterm Infants following Discussions about Withdrawal or Withholding of Life Support. J Pediatr 190:118-123.e4
Younge, Noelle; Goldstein, Ricki F; Bann, Carla M et al. (2017) Survival and Neurodevelopmental Outcomes among Periviable Infants. N Engl J Med 376:617-628

Showing the most recent 10 out of 570 publications